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Chemical Structure Cat. No. Product Name CAS No.
BAY-179 Chemical Structure
BCP49597 BAY-179 2764880-87-5
BAY-179 is a potent, selective, and species cross-reactive OXPHOS complex I inhibitor.
2-Amino-3-methoxypyridine Chemical Structure
BCP12904 2-Amino-3-methoxypyridine 10201-71-5
Telotristat ethyl Chemical Structure
BCP02293 Telotristat ethyl 1033805-22-9
LX1606 is an orally bioavailable, small-molecule, tryptophan hydroxylase (TPH) inhibitor with potential antiserotonergic activity.
RVX-208 Chemical Structure
BCP07787 RVX-208 1044870-39-4
RVX-208 is a first-in-class, small molecule that inhibits BET bromodomains.
6-Fluoroisoquinoline Chemical Structure
BCP02781 6-Fluoroisoquinoline 1075-11-2
Sarecycline Chemical Structure
BCP24790 Sarecycline 1035654-66-0
Sarecycline, also known as WC-3035 and P005672, is a novel, tetracycline-derived, narrow-spectrum antibiotic being developed for use as an oral once daily antibiotic treatment for patients suffering from moderate to severe acne vulgaris.
Tenapanor dihydrochloride Chemical Structure
BCP24893 Tenapanor dihydrochloride 1234365-97-9
Tenapanor, also known as AZD-1722 and RDX 5791, is an inhibitor of the sodium-proton (Na(+)/H(+)) exchanger NHE3, which plays a prominent role in sodium handling in the gastrointestinal tract and kidney.
Branaplam Chemical Structure
BCP19909 Branaplam 1562338-42-4
Branaplam (LMI070) is a highly selective, small-molecule splicing modulators of survival motor neuron‑2 (SMN2) with an EC50 of 0.02 μM.
2H-1-Benzopyran-4-carboxamide, 7-bromo-3,4-dihydro-, (4R)- Chemical Structure
BCP49594 2H-1-Benzopyran-4-carboxamide, 7-bromo-3,4-dihydro-, (4R)- 1851374-84-9
β-Sitosterol Chemical Structure
BCP49592 β-Sitosterol 83-46-5
Beta-Sitosterol is a natural product found in Elodea canadensis, Ophiopogon intermedius, and other organisms with data available.
N-((5-(N-(3-Chlorophenyl)sulfamoyl)-2-methylphenyl)carbamothioyl)-4-fluorobenzamide Chemical Structure
BCP49593 N-((5-(N-(3-Chlorophenyl)sulfamoyl)-2-methylphenyl)carbamothioyl)-4-fluorobenzamide 379696-86-3
MS023 dihydrochloride Chemical Structure
BCP49591 MS023 dihydrochloride 1992047-64-9
MS023 dihydrochloride is a potent, selective, and cell-active inhibitor of human type I protein arginine methyltransferases (PRMTs) inhibitor, with IC50s of 30, 119, 83, 4 and 5 nM for PRMT1, PRMT3, PRMT4, PRMT6, and PRMT8, respectively.
DMCBDA Chemical Structure
BCP49590 DMCBDA 15894-21-0
(S)-1-((S)-2-((2S,3R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)butanamido)-3-(4-methoxyphenyl)propanoyl)-2-methylpyrrolidine-2-car Chemical Structure
BCP49589 (S)-1-((S)-2-((2S,3R)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(tert-butoxy)butanamido)-3-(4-methoxyphenyl)propanoyl)-2-methylpyrrolidine-2-car 2407464-33-7
Coelenterazine H Chemical Structure
BCP10701 Coelenterazine H 50909-86-9
Coelenterazine h is a derivative of Coelenterazine.
BMS-794833 Chemical Structure
BCP02308 BMS-794833 1174046-72-0
BMS 794833 is a potent ATP competitive inhibitor of Met (IC50 = 1.7 nM) and Flk-1 (IC50 = 15 nM).
Landiolol Hydrochloride EnantiomerⅢ Chemical Structure
BCP49588 Landiolol Hydrochloride EnantiomerⅢ 1253907-81-1
Paliperidone Formylation Impurity Chemical Structure
BCP49587 Paliperidone Formylation Impurity 1204315-39-8
Glimepiride sulfonamide Chemical Structure
BCP10472 Glimepiride sulfonamide 119018-29-0
Glimepiride sulfonamide is an intermediate for the preparation of Glimepiride.
Ethyl 5-chloropyrazolo[1,5-a]pyrimidine-3-carboxylate Chemical Structure
BCP14429 Ethyl 5-chloropyrazolo[1,5-a]pyrimidine-3-carboxylate 1224944-77-7
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